证券代码：688336 证券简称：三生国健 公告编号：2025-030 三生国健药业（上海）股份有限公司 2024年年度权益分派实施公告 本公司董事会及全体董事保证公告内容不存在任何虚假记载、误导性陈述或 者重大遗漏，并对其内容的真实性、准确性和完整性依法承担法律责任。 重要内容提示： 每股现金红利0.09元（含税） 相关日期 二、 分配方案 1. 发放年度：2024年年度 | 股权登记日 | 除权（息）日 | 现金红利发放日 | | --- | --- | --- | | 2025/6/12 | 2025/6/13 | 2025/6/13 | 一、 通过分配方案的股东大会届次和日期 本次利润分配方案经公司2025 年 4 月 15日的2024年年度股东大会 审议通过。 是否涉及差异化分红送转：否 每股分配比例 2. 分派对象： 截至股权登记日下午上海证券交易所收市后，在中国证券登记结 算有限责任公司上海分公司（以下简称"中国结算上海分公司"）登记 在册的本公司全体股东。 3. 分配方案： 本次利润分配以方案实施前的公司总股本616,785,793股为基数， 每股派发现金红利0.09元（含税），共计派发现金红 ...

Investment Rating - The report maintains a "Positive" outlook for the pharmaceutical and biotechnology industry in China [6] Core Insights - The ASCO conference showcased significant breakthroughs in both foreign and domestic innovative drugs, highlighting the competitive strength of domestic companies [4][9] - A total of 73 research data entries from domestic companies were included in this year's ASCO, marking a historical high, with 32 being oral presentations and 11 classified as Late-Breaking Abstracts [9][13] - In the NSCLC (non-small cell lung cancer) sector, domestic research is leading globally, with promising data from dual antibodies and ADC (antibody-drug conjugates) [9][10] Summary by Sections Dual Antibodies - PD-1/VEGF dual antibodies are gaining attention, with significant transactions occurring in the market, indicating a heated competition [10][14] - SSGJ-707 from Sanofi has shown impressive efficacy in treating PD-L1 positive advanced NSCLC, with a clinical data showing a cORR of 64.7% and DCR of 97.1% in a specific dosage group [15][16] - PD-1/IL-2, a globally first dual-specific antibody, has demonstrated remarkable efficacy in late-stage NSCLC patients, with a 12-month OS rate of 71.6% [18][19] ADC (Antibody-Drug Conjugates) - ADC combined with immune checkpoint inhibitors is set to replace traditional chemotherapy, with domestic products expected to play a significant role [10][27] - The TROP2 ADC combined with PD-(L)1 has shown promising results in first-line treatment for advanced NSCLC, with an ORR of 55% [27][28] - Sac-TMT from Kelun Biotech has also shown superior efficacy in advanced NSCLC patients, particularly in those with high PD-L1 expression [30][31] Small Cell Lung Cancer (SCLC) - DLL3-targeted therapies have made significant progress, with domestic products demonstrating international competitiveness [10][39] - Tarlatamab has achieved breakthroughs in both second-line and first-line maintenance treatment for SCLC, expanding its indication [10][39] - Domestic DLL3 products have shown promising clinical data, indicating a strong potential for future development [10][39]

Group 1: Market Overview - US stock markets collectively declined, with the Dow Jones down 0.25%, Nasdaq down 0.83%, and S&P 500 down 0.53% [1] - Tesla shares fell by 14.27%, while Nvidia dropped 1.36%, Apple decreased by 1.08%, and Meta Platforms fell by 0.48% [1] - Circle's IPO in the US saw a significant increase of 168% on its first day [1] - Broadcom's Q2 revenue exceeded expectations with a 20% increase, but AI revenue guidance was underwhelming, leading to a post-market drop of over 5% [1] - The Baltic Dry Index rose by 9.2%, marking its seventh consecutive day of increase [1] Group 2: Economic Indicators - The US trade deficit narrowed significantly, with imports dropping by 16.3% [1] - First-time unemployment claims in the US reached 247,000, the highest level since October 2024 [1] Group 3: Domestic Developments - China's Ministry of Commerce announced that it will approve export license applications for rare earths that meet regulations [2] - The Chinese government plans to establish 10 national data factor comprehensive pilot zones to enhance the integration of the digital economy with the real economy [6] Group 4: Industry Insights - The data factor market is projected to grow significantly, with the scale of data assets entering balance sheets expected to increase from 48.7 billion yuan in 2024 to 827.8 billion yuan by 2030, a growth of over 16 times [7] - The Chinese automotive industry is facing increased regulatory scrutiny to maintain fair competition and promote healthy development [8] - The pharmaceutical sector is seeing a shift in the perception of Metformin, which is now being recognized for its potential anti-aging properties, with studies indicating a 30% higher chance of living to 90 for women taking it compared to those on sulfonylureas [8] Group 5: Corporate Announcements - Guokai Microelectronics plans to acquire 94.37% of the shares of Zhongxin Integrated Circuit (Ningbo) [10] - Maipu Medical intends to purchase 100% of Yijie Medical, which will enhance its capabilities in the field of interventional biomaterials [10] - HT Development is planning to acquire a controlling stake in Zhixueyun, which is expected to constitute a major asset restructuring [11]

Group 1 - The National Medical Products Administration (NMPA) has announced a reward system for internal whistleblowers reporting major violations in drug and medical device quality safety, reflecting a commitment to strengthen regulatory oversight in the industry [1] - The introduction of an internal whistleblower incentive mechanism is expected to enhance compliance management among pharmaceutical and medical device manufacturers, promoting long-term healthy development in the industry [1] Group 2 - Sanofi's new drug application for a recombinant anti-IL-1β humanized monoclonal antibody injection for acute gouty arthritis has been accepted by the NMPA, following successful Phase III clinical trials [2] - With over 80 million gout patients in China and a rapid annual growth rate of 9.7%, the market potential for this treatment is significant, and targeting IL-1β is a valuable therapeutic option [2] - The differentiated binding site of the new drug compared to existing products may provide a competitive edge, although its clinical efficacy needs to translate into market competitiveness [2] Group 3 - Zai Lab has signed an exclusive marketing service agreement with Merck's Swiss subsidiary for a recombinant human thyroid-stimulating hormone injection, with a potential maximum authorization fee of RMB 250 million [3] - The agreement includes an initial payment of RMB 50 million and a subsequent payment of RMB 200 million upon approval of the first indication for the product, which is currently in the registration phase [3] - The introduction of this product is expected to fill a gap in the market for post-operative diagnosis of thyroid cancer, leveraging the synergy with Merck's other recommended thyroid medications [3] Group 4 - Maipu Medical has announced plans to acquire 100% equity of Yijie Medical through a combination of share issuance and cash payment, aiming to expand its product offerings into the interventional field [4] - The acquisition is expected to enhance the company's competitive advantage in the research and development of interventional biomaterials and improve marketing efficiency in neurology departments [4] - The company's stock will resume trading on June 6 following the announcement of this acquisition [4]

Group 1 - Hansoh Pharmaceutical granted Regeneron Pharmaceuticals exclusive overseas licensing for its GLP-1/GIP dual receptor agonist HS-20094, which has completed multiple Phase II clinical trials and is currently in Phase III trials in China [1][2] - The licensing agreement includes an upfront payment of $80 million, potential milestone payments of up to $1.93 billion, and double-digit royalties on future sales [2][3] - Recent licensing deals by Chinese pharmaceutical companies indicate a growing trend, with 33 license-out transactions completed in Q1 2025, totaling $36.633 billion, a year-on-year increase of approximately 258% [1][6] Group 2 - The licensing deal with Pfizer for the PD-1/VEGF dual antibody SSGJ-707 includes a record upfront payment of $1.25 billion, with potential milestone payments reaching $4.8 billion [3] - Other companies, such as Sinovant and Ansai, have also announced licensing agreements, indicating a robust market for Chinese pharmaceutical innovations [3][4] - The 2025 ASCO annual meeting showcased over 70 original research results from China, highlighting the international competitiveness of Chinese innovative drugs [4][5] Group 3 - The overall trend shows that Chinese innovative drugs are gaining global value, with a significant increase in licensing transactions and amounts [6][7] - The pharmaceutical industry is expected to see steady recovery, driven by the growing demand for innovative therapies and the improvement in the quality and quantity of domestic innovative drugs [7]

Investment Rating - The report maintains a "Positive" outlook for the pharmaceutical and biotechnology industry in China [6] Core Insights - The ASCO conference showcased significant breakthroughs in both foreign and domestic innovative drugs, highlighting the competitive strength of domestic companies [4][9] - A total of 73 research data entries from domestic companies were included in this year's ASCO, marking a historical high [9][13] - The report emphasizes the potential of dual antibodies and antibody-drug conjugates (ADCs) in the treatment of non-small cell lung cancer (NSCLC) and small cell lung cancer (SCLC) [9][39] Summary by Sections Dual Antibodies - Domestic research is leading globally in dual antibodies, with products like PD-1/VEGF and PD-1/IL-2 showing promise as major drugs in the post-PD-1 era [9][10] - SSGJ-707 from Sanofi has shown impressive efficacy in treating advanced NSCLC, with a clinical data showing a cORR of 64.7% and DCR of 97.1% in specific patient groups [15][16] - IBI363, a first-in-class PD-1/IL-2 dual-specific antibody, has demonstrated significant efficacy in advanced NSCLC, with a median PFS of 9.3 months in squamous cell carcinoma patients [18][19] Antibody-Drug Conjugates (ADCs) - ADCs are expected to gradually replace existing standard of care (SOC) treatments, with domestic products poised to take a significant market share [10][39] - The TROP2 ADC combined with PD-(L)1 therapy has shown promising results in first-line treatment of advanced NSCLC, with an ORR of 55% and mPFS of 11.2 months [27][28] - Sac-TMT from Kelun Biotech has demonstrated superior efficacy compared to Dato-DXd, particularly in patients with high PD-L1 expression [30][31] Small Cell Lung Cancer (SCLC) - DLL3-targeted therapies have made significant progress, with domestic products showing international competitiveness [9][39] - Tarlatamab has achieved breakthroughs in both second-line and first-line maintenance treatment for SCLC, with promising clinical data [9][39] - The report highlights the potential of DLL3-targeted therapies to evolve from dual antibodies to ADCs, enhancing treatment options for SCLC patients [9][39]

证券代码：688336 证券简称：三生国健 公告编号：2025-028 三生国健药业（上海）股份有限公司 2025年第二次临时股东大会决议公告 本公司董事会及全体董事保证公告内容不存在任何虚假记载、误导性陈述或 者重大遗漏，并对其内容的真实性、准确性和完整性依法承担法律责任。 重要内容提示： 本次会议是否有被否决议案：无 一、 会议召开和出席情况 （一） 股东大会召开的时间：2025 年 6 月 5 日 （二） 股东大会召开的地点：中国（上海）自由贸易试验区李冰 路 399 号公司会议室 （三） 出席会议的普通股股东、特别表决权股东、恢复表决权的 优先股股东及其持有表决权数量的情况： | 1、出席会议的股东和代理人人数 | 168 | | --- | --- | | 普通股股东人数 | 168 | | 2、出席会议的股东所持有的表决权数量 | 536,444,676 | | 普通股股东所持有表决权数量 | 536,444,676 | | 3、出席会议的股东所持有表决权数量占公司表决权 | 86.9742 | | 数量的比例（%） | | | --- | --- | | 普通股股东所持有表决权数量占公司表决权数 ...

法律意见书 国浩律师(上海)事务所 法律意见书 致:三生国健药业(上海)股份有限公司 根据《中华人民共和国公司法》(以下简称"《公司法》")、《中华人民 共和国证券法》(以下简称"《证券法》")和中国证券监督管理委员会《上市 公司股东会规则》（以下简称"《股东会规则》"）的规定,国浩律师（上海) 事务所接受三生国健药业(上海)股份有限公司(以下简称"公司")董事会的 聘请,指派律师现场见证了公司于 2025年 6 月 5 日 10:00 起在中国(上海)自由 贸易试验区李冰路 399 号公司会议室召开的公司 2025年第二次临时股东大会,并 依据有关法律、法规、规范性文件的规定以及《三生国健药业(上海)股份有限 公司章程》(以下简称"《公司章程》")的规定,对本次股东大会的召集、召 开程序、出席人员资格、大会表决程序等事宜进行了审查,现发表法律意见如下: 国浩律师(上海)事务所 一、股东大会的召集、召开程序 关于三生国健药业(上海)股份有限公司 公司董事会已于 2025 年 5 月 21 日在中国证监会指定信息披露网站上向公司 股东发出了召开 2025年第二次临时股东大会的会议通知。经核查,相关通知及公 告载 ...

近日，三生国健药业（上海）股份有限公司（以下简称"公司" 或"三生国健"）重组抗 IL-1β人源化单克隆抗体注射液（项目代 号"SSGJ-613"）用于急性痛风性关节炎适应症的 III 期临床试验达 到了主要疗效双终点，公司向国家药品监督管理局（NMPA）药品审评 中心（CDE）提交了新药上市申请并获得受理。 证券代码： 688336 证券简称：三生国健 公告编号：2025-029 三生国健药业（上海）股份有限公司 关于自愿披露公司重组抗 IL-1β人源化单克隆抗体 注射液新药上市申请获得受理的公告 本公司董事会及全体董事保证本公告内容不存在任何虚假记载、误导性陈述 或者重大遗漏，并对其内容的真实性、准确性和完整性依法承担法律责任。 重要内容提示： 由于新药上市申请尚需经过审评、药品临床试验现场检查、药品 生产现场检查和审批等环节，产品能否成功上市及上市时间存在不确 定性。敬请广大投资者谨慎决策，注意防范投资风险。 现将相关情况公告如下： | 药品名称 | 重组抗 IL-1β人源化单克隆抗体注射液 | | --- | --- | | 剂型 | 注射剂 | | 申请事项 | 境内生产药品注册上市许可 | 一、药 ...

Core Viewpoint - Sanofi's application for the new drug SSGJ-613, a recombinant humanized monoclonal antibody targeting IL-1β for acute gouty arthritis, has been accepted by the National Medical Products Administration after achieving primary efficacy endpoints in Phase III clinical trials [1] Group 1 - The drug SSGJ-613 is developed independently by the company and represents a novel anti-IL-1β antibody with a completely different binding epitope compared to existing products on the market targeting the same pathway [1]